Canonical Allele Identifier: CA2319224446

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099380T= , CM000681.2:g.4099380T=	GRCh38
NC_000019.9:g.4099378T= , CM000681.1:g.4099378T=	GRCh37
NC_000019.8:g.4050378T=	NCBI36
NG_007996.1:g.29749A= , LRG_750:g.29749A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1179A=
ENST00000687128.1:n.1179A=
ENST00000688002.1:n.1034A=
ENST00000689792.1:n.646-2A=
ENST00000262948.10:c.740A= MANE Select	ENSP00000262948.4:p.Gln247=
ENST00000262948.9:c.740A=	ENSP00000262948.3:p.Gln247=
ENST00000394867.8:c.449A=	ENSP00000378336.1:p.Gln150=
ENST00000593364.5:n.687A=
ENST00000595715.1:n.555A=
ENST00000597263.5:n.169+1639A=
ENST00000599021.1:c.29+1639A=
ENST00000600584.5:n.1300A=
ENST00000601786.5:n.1041A=
NM_030662.3:c.740A= , LRG_750t1:c.740A=	NP_109587.1:p.Gln247=
XM_006722799.2:c.705+1639A=	XP_006722862.1:n.705+1639A=
XM_011528133.1:c.170A=	XP_011526435.1:p.Gln57=
XM_017026989.1:c.740A=	XP_016882478.1:p.Gln247=
XM_017026990.1:c.705+1639A=	XP_016882479.1:n.705+1639A=
NM_030662.4:c.740A= MANE Select	NP_109587.1:p.Gln247=